HGVS | Genome Assembly |
---|---|
NC_000006.12:g.31861434A>G , CM000668.2:g.31861434A>G | GRCh38 |
NC_000006.11:g.31829211A>G , CM000668.1:g.31829211A>G | GRCh37 |
NC_000006.10:g.31937190A>G | NCBI36 |
NG_008201.1:g.6499T>C | |
NG_023058.1:g.22613T>C |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000375631.5:c.369T>C MANE Select | ENSP00000364782.4:p.Pro123= | |
ENST00000677054.1:n.1046T>C | ||
ENST00000677512.1:n.477T>C | ||
ENST00000678869.1:n.477T>C | ||
ENST00000375631.4:c.369T>C | ENSP00000364782.4:p.Pro123= | |
ENST00000480384.1:n.398T>C | ||
ENST00000491768.5:c.369T>C | ENSP00000433127.1:p.Pro123= | |
ENST00000495807.1:n.937T>C | ||
NM_000434.3:c.369T>C | NP_000425.1:p.Pro123= | |
NM_000434.4:c.369T>C MANE Select | NP_000425.1:p.Pro123= |